rs5921979
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs5921979(C;C) |
| Make rs5921979(C;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | X |
| Position | 83509034 |
| Gene | POU3F4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5921979 |
| dbSNP (classic) | rs5921979 |
| ClinGen | rs5921979 |
| ebi | rs5921979 |
| HLI | rs5921979 |
| Exac | rs5921979 |
| Gnomad | rs5921979 |
| Varsome | rs5921979 |
| LitVar | rs5921979 |
| Map | rs5921979 |
| PheGenI | rs5921979 |
| Biobank | rs5921979 |
| 1000 genomes | rs5921979 |
| hgdp | rs5921979 |
| ensembl | rs5921979 |
| geneview | rs5921979 |
| scholar | rs5921979 |
| rs5921979 | |
| pharmgkb | rs5921979 |
| gwascentral | rs5921979 |
| openSNP | rs5921979 |
| 23andMe | rs5921979 |
| SNPshot | rs5921979 |
| SNPdbe | rs5921979 |
| MSV3d | rs5921979 |
| GWAS Ctlg | rs5921979 |
| GMAF | 0.1076 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs5921979(C;C) |
| Alt | rs5921979(C;C) |
| Reference | Rs5921979(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | POU3F4 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000023.10:g.82764042G>C |
| CLNSRC | ClinVar |
| CLNACC | RCV000036257.2, |
